Canonical Allele Identifier: CA1539568866
Gene: NIPBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36975777C= , CM000667.2:g.36975777C= GRCh38
NC_000005.9:g.36975879C= , CM000667.1:g.36975879C= GRCh37
NC_000005.8:g.37011636C= NCBI36
NG_006987.1:g.103895C=
NG_006987.2:g.103895C=

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.870C= MANE Select ENSP00000282516.8:p.Gly290=
ENST00000652901.1:c.870C= ENSP00000499536.1:p.Gly290=
ENST00000282516.12:c.870C= ENSP00000282516.8:p.Gly290=
ENST00000448238.2:c.870C= ENSP00000406266.2:p.Gly290=
ENST00000504430.5:n.490C=
ENST00000505998.5:n.849C=
ENST00000621733.1:c.1-88801C= ENSP00000480694.1:n.1-88801C=
NM_015384.4:c.870C= NP_056199.2:p.Gly290=
NM_133433.3:c.870C= NP_597677.2:p.Gly290=
XM_005248280.2:c.870C= XP_005248337.1:p.Gly290=
XM_005248282.3:c.126C= XP_005248339.2:p.Gly42=
XM_006714467.2:c.870C= XP_006714530.1:p.Gly290=
XM_006714468.1:c.870C= XP_006714531.1:p.Gly290=
XM_011514014.1:c.870C= XP_011512316.1:p.Gly290=
XM_011514015.1:c.870C= XP_011512317.1:p.Gly290=
XM_005248280.3:c.870C= XP_005248337.1:p.Gly290=
XM_005248282.5:c.210C= XP_005248339.3:p.Gly70=
XM_006714468.2:c.870C= XP_006714531.1:p.Gly290=
XM_017009329.1:c.870C= XP_016864818.1:p.Gly290=
XM_017009331.1:c.870C= XP_016864820.1:p.Gly290=
NM_133433.4:c.870C= MANE Select NP_597677.2:p.Gly290=
NM_015384.5:c.870C= NP_056199.2:p.Gly290=